TY - JOUR
T1 - Thymic stromal lymphopoietin is a key mediator of breast cancer progression
AU - Olkhanud, Purevdorj B.
AU - Rochman, Yrina
AU - Bodogai, Monica
AU - Malchinkhuu, Enkhzol
AU - Wejksza, Katarzyna
AU - Xu, Mai
AU - Gress, Ronald E.
AU - Hesdorffer, Charles
AU - Leonard, Warren J.
AU - Biragyn, Arya
PY - 2011/5/15
Y1 - 2011/5/15
N2 - Inflammation is a double-edged sword that can promote or suppress cancer progression. In this study, we report that thymic stromal lymphopoietin (TSLP), an IL-7 - like type 1 inflammatory cytokine that is often associated with the induction of Th2-type allergic responses in the lungs, is also expressed in human and murine cancers. Our studies with murine cancer cells indicate that TSLP plays an essential role in cancer escape, as its inactivation in cancer cells alone was sufficient to almost completely abrogate cancer progression and lung metastasis. The cancer-promoting activity of TSLP primarily required signaling through the TSLP receptor on CD4+ T cells, promoting Th2-skewed immune responses and production of immunosuppressive factors such as IL-10 and IL-13. Expression of TSLP therefore may be a useful prognostic marker, and its targeting could have therapeutic potential.
AB - Inflammation is a double-edged sword that can promote or suppress cancer progression. In this study, we report that thymic stromal lymphopoietin (TSLP), an IL-7 - like type 1 inflammatory cytokine that is often associated with the induction of Th2-type allergic responses in the lungs, is also expressed in human and murine cancers. Our studies with murine cancer cells indicate that TSLP plays an essential role in cancer escape, as its inactivation in cancer cells alone was sufficient to almost completely abrogate cancer progression and lung metastasis. The cancer-promoting activity of TSLP primarily required signaling through the TSLP receptor on CD4+ T cells, promoting Th2-skewed immune responses and production of immunosuppressive factors such as IL-10 and IL-13. Expression of TSLP therefore may be a useful prognostic marker, and its targeting could have therapeutic potential.
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U2 - 10.4049/jimmunol.1100463
DO - 10.4049/jimmunol.1100463
M3 - Article
C2 - 21490155
AN - SCOPUS:79956194490
SN - 0022-1767
VL - 186
SP - 5656
EP - 5662
JO - Journal of Immunology
JF - Journal of Immunology
IS - 10
ER -